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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257162Generated: October 26, 2026

Sodium borohydride → N-(4-chloro-2-fluoro-3-(hydroxymethyl)phenyl)acetamide

https://huagongshe.com/reaction/1257162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantN-(4-chloro-2-fluoro-3-formylphenyl)acetamideHCID 84784262—
SolventMethanolHCID 887—
ProductN-(4-chloro-2-fluoro-3-(hydroxymethyl)phenyl)acetamideHCID 8671362595%

Reaction Conditions

Temperature0 °C

Reaction Steps

A 0° C. solution of N-(4-chloro-2-fluoro-3-formylphenyl)acetamide (1.1 g, 5.10 mmol) in MeOH (10 mL) was treated portion-wise with sodium borohydride (0.193 g, 5.10 mmol), stirred at 0° C. for 0.5 h, then warmed to RT and concentrated to dryness. The residue was treated with water, extracted with EtOAc (2×) and the combined organics were washed with brine, dried over Na2SO4 and concentrated to dryness to afford N-(4-chloro-2-fluoro-3-(hydroxymethyl)phenyl)acetamide (1.05 g, 95% yield) as a white solid. MS (ESI) m/z: 218.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461179B1
Source datasetuspto-grants-2013_06
ORD IDord-b0bb77f9e9324c4a86b06e5b1e90468a
Source noteuspto-grants-2013_06